Mindray DS USA, Inc. dba Mindray North America recalls
3 recalls on record · FDA
Every recall we have on record for Mindray DS USA, Inc. dba Mindray North America, compiled from federal safety data. Check the hazard, the remedy, and how serious each one is, and always confirm on the official notice.
Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as…
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to…
V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention
Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia System-Used to provide the…
V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention